Wolf-Hirschhorn syndrome has 19 match(es) New Search



Wolf-Hirschhorn syndrome

A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a microdeletion of the short arm of chromosome 4.

4p deletion syndrome, chromosome 4p16.3 deletion syndrome, PITT SYNDROME, Pitt-Rogers-Danks Syndrome

OMIM:194190

Morpholino Experiments
letm1 MO1 Xla Wt + letm1 MO  Xla Wt + letm1 MO 
nelfa MO1 Xla Wt + nelfa MO  Xla Wt + nelfa MO  Xla Wt + nelfa MO  Xla Wt + nelfa MO 
nsd2 MO1 Xla Wt + nsd2 MO  Xla Wt + nsd2 MO  Xla Wt + nsd2 MO  Xla Wt + nsd2 MO 
tacc3 MO2 Xla Wt + tacc3 MO  Xla Wt + tacc3 MO  Xla Wt + tacc3 MO  Xla Wt + tacc3 MO  Xla Wt + tacc3 MO